Canonical Allele Identifier: CA2479571489

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151408446_151408448delinsCAG , CM000663.2:g.151408446_151408448delinsCAG	GRCh38
NC_000001.10:g.151380922_151380924delinsCAG , CM000663.1:g.151380922_151380924delinsCAG	GRCh37
NC_000001.9:g.149647546_149647548delinsCAG	NCBI36
NG_046601.1:g.56018_56020delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000710270.1:c.2243_2245delinsCTG	ENSP00000518163.1:p.Pro748=
ENST00000392723.6:c.2036_2038delinsCTG	ENSP00000376484.1:p.Pro679=
ENST00000439756.2:c.2195_2197delinsCTG	ENSP00000390156.2:p.Pro732=
ENST00000703168.1:c.2216_2218delinsCTG	ENSP00000515214.1:p.Pro739=
ENST00000271715.7:c.2195_2197delinsCTG MANE Select	ENSP00000271715.2:p.Pro732=
ENST00000271715.6:c.2195_2197delinsCTG	ENSP00000271715.2:p.Pro732=
ENST00000358476.7:n.2064_2066delinsCTG
ENST00000368863.6:c.1910_1912delinsCTG	ENSP00000357856.2:p.Pro637=
ENST00000392723.5:c.2036_2038delinsCTG	ENSP00000376484.1:p.Pro679=
ENST00000409503.5:c.2168_2170delinsCTG	ENSP00000386836.1:p.Pro723=
ENST00000491586.5:c.2063_2065delinsCTG	ENSP00000418408.1:p.Pro688=
ENST00000492528.1:n.106_108delinsCTG
ENST00000529669.1:c.395_397delinsCTG	ENSP00000432295.1:p.Pro132=
ENST00000531094.5:c.2009_2011delinsCTG	ENSP00000431259.1:p.Pro670=
NM_001194937.1:c.2168_2170delinsCTG	NP_001181866.1:p.Pro723=
NM_001194938.1:c.2009_2011delinsCTG	NP_001181867.1:p.Pro670=
NM_015100.3:c.2195_2197delinsCTG	NP_055915.2:p.Pro732=
NM_145796.3:c.1910_1912delinsCTG	NP_665739.3:p.Pro637=
NM_207171.2:c.2036_2038delinsCTG	NP_997054.1:p.Pro679=
XM_005244999.1:c.2195_2197delinsCTG	XP_005245056.1:p.Pro732=
XM_005245000.3:c.2195_2197delinsCTG	XP_005245057.1:p.Pro732=
XM_005245001.1:c.2195_2197delinsCTG	XP_005245058.1:p.Pro732=
XM_005245005.1:c.2036_2038delinsCTG	XP_005245062.1:p.Pro679=
XM_005245006.3:c.2036_2038delinsCTG	XP_005245063.1:p.Pro679=
XM_011509330.1:c.2087_2089delinsCTG	XP_011507632.1:p.Pro696=
XM_011509331.1:c.1838_1840delinsCTG	XP_011507633.1:p.Pro613=
XR_921760.1:n.2063-208_2063-206delinsCTG
XM_005244999.3:c.2195_2197delinsCTG	XP_005245056.1:p.Pro732=
XM_005245000.4:c.2195_2197delinsCTG	XP_005245057.1:p.Pro732=
XM_005245001.2:c.2195_2197delinsCTG	XP_005245058.1:p.Pro732=
XM_005245005.2:c.2036_2038delinsCTG	XP_005245062.1:p.Pro679=
XM_005245006.5:c.2036_2038delinsCTG	XP_005245063.1:p.Pro679=
XM_017000744.1:c.2216_2218delinsCTG	XP_016856233.1:p.Pro739=
XM_017000745.2:c.2168_2170delinsCTG	XP_016856234.1:p.Pro723=
XM_017000746.1:c.2168_2170delinsCTG	XP_016856235.1:p.Pro723=
XM_017000748.1:c.2036_2038delinsCTG	XP_016856237.1:p.Pro679=
XM_017000749.1:c.2036_2038delinsCTG	XP_016856238.1:p.Pro679=
XM_024454305.1:c.2069_2071delinsCTG	XP_024310073.1:p.Pro690=
XM_024454306.1:c.995_997delinsCTG	XP_024310074.1:p.Pro332=
XR_002959801.1:n.2090-208_2090-206delinsCTG
NM_015100.4:c.2195_2197delinsCTG MANE Select	NP_055915.2:p.Pro732=
NM_001194937.2:c.2168_2170delinsCTG	NP_001181866.1:p.Pro723=
NM_001194938.2:c.2009_2011delinsCTG	NP_001181867.1:p.Pro670=
NM_145796.4:c.1910_1912delinsCTG	NP_665739.3:p.Pro637=